Synthesis of (24R)- and (24S)-5,28-stigmastadien-3.beta.-ol and determination of the stereochemistry of their 24-hydroxy analogs, the saringosterols
- 1 December 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 48 (26) , 5207-5214
- https://doi.org/10.1021/jo00174a011
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Synthesis of (24R,28R)- and (24S,28S)-fucosterol epoxides. Revision of C-24,28 configurationsThe Journal of Organic Chemistry, 1980
- Dinosterol side chain biosynthesis in a marine dinoflagellate, Crypthecodinium cohniiPhytochemistry, 1979
- Minor and trace sterols in marine invertebrates. 8. Isolation, structure elucidation, and partial synthesis of two novel sterols - stelliferasterol and isostelliferasterolJournal of the American Chemical Society, 1978
- Investigations on the ring contraction step in the biosynthesis of A-nor-stanols by the marine sponge Axinella verrucosaJournal of the Chemical Society, Chemical Communications, 1978
- Electron impact induced fragmentation of cholesterol and related C-5 unsaturated steroidsThe Journal of Organic Chemistry, 1977
- Check-list of British marine algae-third revisionJournal of the Marine Biological Association of the United Kingdom, 1976